检索结果 - Korcan Demir

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  1. 1
    Genetic Causes of Rickets

    Genetic Causes of Rickets 由 Sezer Acar, Korcan Demir, Yufei Shi

    出版 2018
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  2. 2
    The Role of Initial Clinical and Laboratory Findings in Infants With Hyperthyrotropinemia to Predict Transient or Permanent Hypothyroidism

    The Role of Initial Clinical and Laboratory Findings in Infants With Hyperthyrotropinemia to Predict Transient or Permanent Hypothyroidism 由 Ünüvar Tolga, Korcan Demir, Abacı Ayhan, Büyükgebiz Atilla, Böber Ece

    出版 2013
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  3. 3
    A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics

    A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics 由 Korcan Demir, Samim Özen, Ergun Konakçı, Murat Aydın, Feyza Darendelıler

    出版 2017
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  4. 4
    Has the Frequency of Precocious Puberty and Rapidly Progressive Early Puberty Increased in Girls During the COVID-19 Pandemic?

    Has the Frequency of Precocious Puberty and Rapidly Progressive Early Puberty Increased in Girls During the COVID-19 Pandemic? 由 Kübra Yüksek Acınıklı, İbrahim Mert Erbaş, Özge Besci, Korcan Demir, Ayhan Abacı, Ece Böber

    出版 2022
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  5. 5
    New Features for Child Metrics: Further Growth References and Blood Pressure Calculations

    New Features for Child Metrics: Further Growth References and Blood Pressure Calculations 由 Korcan Demir, Ergun Konakçı, Güven Özkaya, Belde Kasap Demir, Samim Özen, Murat Aydın, Feyza Darendelıler

    出版 2019
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  6. 6
    Single sural nerve response: A reliable and practical method for diagnosis of diabetic peripheral neuropathy in children with type 1 diabetes

    Single sural nerve response: A reliable and practical method for diagnosis of diabetic peripheral neuropathy in children with type 1 diabetes 由 Hüseyin Bahadır Şenol, Özge Yıldırım Şalbaş, Elif Naz Kadem, Mustafa Halk, Ayşe İpek Polat, Adem Aydın, Semra Hız Kurul, Korcan Demir, Uluç Yiş

    出版 2025
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  7. 7
    Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A

    Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A 由 Korcan Demir, Walaa E. Kattan, Minjing Zou, Erdem Durmaz, Huda A. BinEssa, Özlem Nalbantoğlu, Roua A. Al‐Rijjal, Brian F. Meyer, Behzat Özkan, Yufei Shi

    出版 2015
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  8. 8
    What is the Most Effective Method for Predicting Adult Height in Boys with Constitutional Delay of Growth and Puberty?

    What is the Most Effective Method for Predicting Adult Height in Boys with Constitutional Delay of Growth and Puberty? 由 Gözde Akın Kağızmanlı, Deniz Özalp Kızılay, Reyhan Deveci Sevim, Kübra Yüksek Acinikli, Fulya Mete Kalaycı, Ayşegül Tekneci, Korcan Demir, Ece Böber, Ahmet Anık, Samim Özen, Ayhan Abacı

    出版 2025
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  9. 9
    Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

    Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations 由 Korcan Demir, Anja L.M. van Gucht, Muammer Büyükinan, Gönül Çatlı, Yavuz Ayhan, Veysel Nijat Baş, Bumin Nuri Dündar, Behzat Özkan, Marcel E. Meima, W. Edward Visser, Robin P. Peeters, Theo J. Visser

    出版 2016
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  10. 10
    Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress

    Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress 由 Hossam Montaser, Kashyap Patel, Diego Balboa, Hazem Ibrahim, Väinö Lithovius, Anna Näätänen, Vikash Chandra, Korcan Demir, Sezer Acar, Tawfeg Ben‐Omran, Kevin Colclough, Jonathan M. Locke, Matthew N. Wakeling, Maria Lindahl, Andrew T. Hattersley, Jonna Saarimäki‐Vire, Timo Otonkoski

    出版 2021
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  11. 11
    Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review

    Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review 由 Özge Besci, Maria Cristina Foss‐Freitas, Natália Rossin Guidorizzi, Merve Çelik Güler, Donatella Gilio, Jessica N. Maung, Rebecca L. Schill, Keegan S. Hoose, Bonje Obua, ANABELA DILL GOMES, İlgın Yıldırım Şimşir, Korcan Demir, Barış Akıncı, Ormond A. MacDougald, Elif A Oral

    出版 2023
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  12. 12
    Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

    Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome 由 Katherina Walz, Devon Cohen, Paul M. Neilsen, Joseph Foster, Francesco Brancati, Korcan Demir, Richard Fisher, Michelle Moffat, Nienke E. Verbeek, Kathrine Bjørgo, Adriana Lo Castro, Paolo Curatolo, Giuseppe Novelli, Clemer Abad, Lei Cao, Lily Zhang, Oscar Diaz‐Horta, Juan I. Young, David F. Callen, Mustafa Tekin

    出版 2014
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  13. 13
    Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

    Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study 由 Gökşen Damla, Aycan Zehra, Samim Özen, Çetinkaya Semra, Kara Cengiz, Saygın Abalı, Korcan Demir, Tunç Özgül, Seyit Ahmet Uçaktürk, Asar Gülgün, Baş Firdevs, Çetinkaya Ergun, A. Murat, Karagüzel Gülay, Orbak Zerrin, Zeynep Şıklar, Altıncık Ayça, Ökten Ayşenur, Özkan Behzat, Öçal Gönül, Serap Semiz, Arslanoğlu İlknur, Evliyaoğlu Olcay, Bundak Rüveyde, Darcan Şükran

    出版 2013
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  14. 14
    7756 Gonadectomy in Individuals with Differences of Sex Development - A Prospective I-DSD Registry Study

    7756 Gonadectomy in Individuals with Differences of Sex Development - A Prospective I-DSD Registry Study 由 Michele Ann O'Connell, Angela K Lucas‐Herald, Jillian Bryce, Minglu Chen, Justin H. Davies, Margarett Shnorhavorian, Navoda Atapattu, Inna Bachynska, Niels Birkebæk, Martine Cools, Korcan Demir, Liat de Vries, Heba Elsedfy, Mohamed Abdelsabour Fahmy, Evgenia Globa, Romina P. Grinspon, Guilherme Guaragna‐Filho, Gil Guerra‐Júnior, Dominika Januś, Zofia Kolesińska, Inas Mazen, Susan O’Çonnell, Sumudu Nimali Seneviratne, Marianna Rita Stancampiano, Gilvydas Verkauskas, S. Faisal Ahmed

    出版 2024
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  15. 15
    Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

    Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort 由 Tülay Güran, Federica Buonocore, Nurçin Saka, Mehmet Nuri Özbek, Zehra Aycan, Abdullah Bereket, Firdevs Baş, Şükran Darcan, Aysun Bıdecı, Ayla Güven, Korcan Demir, Ayşehan Akıncı, Muammer Büyükinan, Banu Küçükemre Aydın, Serap Turan, Sebahat Yılmaz Ağladıoğlu, Zeynep Atay, Zehra Yavaş Abalı, Ömer Tarım, Gönül Çatlı, Bilgin Yüksel, Teoman Akçay, Metin Yıldız, Samim Özen, Esra Döğer, Hüseyin Demirbilek, Ahmet Uçar, Emregül Işık, Bayram Özhan, Semih Bolu, İlker Tolga Özgen, Jenifer P. Suntharalingham, John C. Achermann

    出版 2015
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  16. 16
    Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

    Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study 由 Ediz Yeşilkaya, Abdullah Bereket, Feyza Darendelıler, Firdevs Baş, Şükran Poyrazoğlu, Banu Küçükemre Aydın, Şükran Darcan, Bumin Nuri Dündar, Muammer Büyükinan, Cengiz Kara, Erkan Sarı, Erdal Adal, Ayşehan Akıncı, Mehmet Emre Atabek, Fatma Demirel, Nurullah Çelik, Behzat Özkan, Bayram Özhan, Zerrin Orbak, Betül Ersoy, Murat Doğan, Ali Ataş, Serap Turan, Damla Gökşen, Ömer Tarım, Bilgin Yüksel, Oya Ercan, Şükrü Hatun, Enver Şimşek, Ayşenur Ökten, Ayhan Abacı, Hakan Döneray, Mehmet Nuri Özbek, Mehmet Keskın, Hasan Önal, Nesibe Akyürek, Kezban Bulan, Derya Tepe, Hamdi Cihan Emeksiz, Korcan Demir, Deniz Özalp Kızılay, A. Kemal Topaloğlu, Erdal Eren, Samim Özen, Saygın Abalı, Leyla Akın, Beray Selver Eklioğlu, Sultan Kaba, Ahmet Anık, Serpil Baş, Tolga Ünüvar, Halil Sağlam, Semih Bolu, İlker Tolga Özgen, Durmuş Doğan, Esra Deniz Papatya Çakır, Yaşar Şen, Nesibe Andıran, Filiz Çizmecioğlu, Olcay Evliyaoğlu, Gülay Karagüzel, Özgür Pirgon, Gönül Çatlı, Hatice Dilek Can, Fatih Gürbüz, Çiğdem Binay, Veysel Nijat Baş, Kürşat Fidancı, Adem Polat, Davut Gül, Cengizhan Açıkel, Hüseyin Demirbilek, Peyamı Cınaz, Carolyn A. Bondy

    出版 2015
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  17. 17
    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study 由 Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı, Alberto Alcantud, Gautam Ambegaonkar, Christine M. Armour, Priyanka Bakhtiani, Diana Bârcă, Enrico Bertini, Ingrid M. van Beynum, Nicola Brunetti‐Pierri, Marianna Bugiani, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Claudia Castiglioni, Krishna Chatterjee, I.F.M. de Coo, Régis Coutant, Dana Craiu, Patricia Crock, Christian DeGoede, Korcan Demir, Alice Dica, Paul Dimitri, Anna Dolcetta‐Capuzzo, Marjolein H. G. Dremmen, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Belinda George, Evelien Gevers, Annette Hackenberg, Zita Halász, Bianka Heinrich, Tony Huynh, Anna Kłosowska, Marjo S. van der Knaap, Marieke M van der Knoop, Daniel Konrad, David A. Koolen, Heiko Krude, Amy Lawson‐Yuen, Jan Lebl, M Linder-Lucht, Cláudia Fernandes Lorea, Charles Marques Lourenço, Roelineke J. Lunsing, Greta Lyons, Jana Malíková, Edna E. Mancilla, Anne McGowan, Verónica Mericq, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Isabelle Oliver‐Petit, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Fabiano O. Poswar, Christina Reinauer, Klára Roženková, tuba seven menevse, Peter Simm, Anna Simon, Yogen Singh, Marco Spada, Jet van der Spek, Milou A.M. Stals, Athanasia Stoupa, Gopinath M. Subramanian, Davide Tonduti, Serap Turan, Corstiaan A. den Uil, Joel A. Vanderniet, Adri van der Walt, Jean‐Louis Wémeau, Jolante Wierzba, Marie‐Claire Y. de Wit, Nicole I. Wolf, Michael Wurm, Federica Zibordi, Amnon Zung, Nitash Zwaveling‐Soonawala, W. Edward Visser

    出版 2020
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  18. 18
    Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration

    Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration 由 Stefan Groeneweg, Ferdy S. van Geest, Mariano Martín, Mafalda Dias, Jonathan Frazer, Carolina Medina‐Gómez, Rosalie Sterenborg, Hao Wang, Anna Dolcetta‐Capuzzo, Linda J. de Rooij, Alexander Teumer, Ayhan Abacı, Erica L T van den Akker, Gautam Ambegaonkar, Christine M. Armour, I. Bacos, Priyanka Bakhtiani, Diana Bârcă, Andrew J. Bauer, Sjoerd A.A. van den Berg, Amanda van den Berge, Enrico Bertini, Ingrid M. van Beynum, Nicola Brunetti‐Pierri, Doris Brunner, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Claudia Castiglioni, Krishna Chatterjee, Alexander Chesover, Peter Christian, Jet van der Spek, I.F.M. de Coo, R. Coutant, Dana Craiu, Patricia Crock, Christian de Goede, Korcan Demir, Cheyenne Dewey, Alice Dica, Paul Dimitri, Marjolein H. G. Dremmen, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Luigi Garibaldi, Belinda George, Evelien Gevers, Erin Greenup, Annette Hackenberg, Zita Halász, Bianka Heinrich, Anna Hurst, Tony Huynh, Amber Isaza, Anna Kłosowska, Marieke M van der Knoop, Daniel Konrad, David A. Koolen, Heiko Krude, Abhishek Kulkarni, Alexander Laemmle, Stephen LaFranchi, Amy Lawson‐Yuen, Jan Lebl, Selmar Leeuwenburgh, M Linder-Lucht, Amelia Martí, Cláudia Fernandes Lorea, Charles Marques Lourenço, Roelineke J. Lunsing, Greta Lyons, Jana Malíková, Edna E. Mancilla, Kenneth McCormick, Anne McGowan, Verónica Mericq, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Lindsey Nicol, Isabelle Oliver‐Petit, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Fabiano de Oliveira Poswar, Christina Reinauer, Klára Roženková, Rowen Seckold, tuba seven menevse, Peter Simm, Anna Simon, Yogen Singh, Marco Spada, Milou A.M. Stals, Merel T Stegenga, Athanasia Stoupa

    出版 2025
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